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Polysaccharide vaccines as probes of antibody repertoires in man
Author(s) -
Lucas Alexander H.,
Reason Donald C.
Publication year - 1999
Publication title -
immunological reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.839
H-Index - 223
eISSN - 1600-065X
pISSN - 0105-2896
DOI - 10.1111/j.1600-065x.1999.tb01343.x
Subject(s) - biology , germline , immunogen , somatic hypermutation , population , epitope , antibody , antibody repertoire , immunoglobulin idiotypes , acquired immune system , antigen , immunity , immunology , genetics , repertoire , germline mutation , virology , idiotype , gene , immune system , mutation , monoclonal antibody , b cell , medicine , physics , environmental health , acoustics
Summary: Antibodies specific for capsular polysaccharide epitopes mediate immunity to encapsulated bacterial pathogens, and accordingly, vac‐cine development has focused upon the induction of these specificities. Efficacious vaccines, consisting of either polysaccharide alone or polysaccharide coupled to protein carriers, have been developed for a number of pathogens. Their clinical importance not with standing, these vaccines serve as model antigens to study the genetic and somatic forces molding adaptive immunity in man. In this article we review progress aimed at delineating the structure and dynamics of the human antibody repertoire to the Hoemophilus influenzoe type b poiysaccharide (Hib PS), a system which has been studied from infancy to old age. Collectively, the data reveal a repertoire which is encoded by a relatively iarge number of germline variable (V) region gene segments, but which is typically expressed within individuals as a markedly restricted, oligoclonal population. One particular V domain has attained canonical status because of its high penetrance at the population level and its predominance in individual repertoires, Although this combining site is assembled in early infancy and retains its prominence throughout life, its frequency of expression, affinity and protective function are dictated by the molecular form of the Hib PS immunogen (vaccine). The determinants of Hib PS binding affinity can include both germline and somatically‐acquired V region polymorphisms. We discuss how these properties of the Hib PS repertoire could impact immunity to Htb, and we consider the implications of these findings towards understanding die evolution of immunoglobulin germline V genes.